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成人型酸性麦芽糖酶缺乏症。一个家族中临床及病理异常的分布与进展情况

Adult onset acid maltase deficiency. Distribution and progression of clinical and pathological abnormality in a family.

作者信息

Swash M, Schwartz M S, Apps M C

出版信息

J Neurol Sci. 1985 Apr;68(1):61-74. doi: 10.1016/0022-510x(85)90050-4.

Abstract

The adult onset form of acid maltase deficiency (Type IIb) clinically affects only skeletal muscle. Proximal weakness is more severe in legs than arms and involvement of respiratory muscles is prominent in about a third of the cases. In three siblings with the disease, the severity of limb weakness was related to age and duration of disease. Respiratory muscle involvement was a feature in two of the patients. The pathological abnormality was more marked in quadriceps than deltoid, and was strikingly patchy in distribution within these muscles. In one case, vacuolar change was not evident by light microscopy in two quadriceps biopsies taken 2 years apart. There is thus a spectrum of clinical and pathological expression of the disorder even in a single sibship.

摘要

成人起病型酸性麦芽糖酶缺乏症(IIb型)临床上仅累及骨骼肌。近端肌无力在腿部比手臂更严重,约三分之一的病例中呼吸肌受累明显。在三名患有该疾病的兄弟姐妹中,肢体无力的严重程度与年龄和病程有关。两名患者有呼吸肌受累表现。病理异常在股四头肌比三角肌更明显,且在这些肌肉内分布明显呈斑片状。在一个病例中,相隔2年采集的两份股四头肌活检标本,光镜下均未发现空泡样改变。因此,即使在单个家族中,该疾病也存在一系列临床和病理表现。

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